Coating compositions from oil modified polyurethane dispersions
Low VOC compositions for coating, staining and protecting porous substrates such as wood, concrete, cement, brick and the like, comprising aqueous dispersions of polyurethane-ureas.
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Claims
1. A composition comprising a dispersion of a polyurethane-urea in an aqueous media having a particle size diameter of less than about 0.4 micron; wherein the polyurethane-urea dispersion is obtained by dispersing, in the presence of a weak base, an isocyanate functional prepolymer into water and admixing a diamine chain extender, wherein the prepolymer is formed by reacting in the presence of a catalyst:
- (i) an active-hydrogen containing composition containing at least two active hydrogen groups per molecule:
- (ii) an isocyanate-functional material; and
- (iii) a modifier composition selected from the group consisting of C6-C22 aliphatic chain-containing anhydride-functional fatty acids and oils, and mixtures thereof,
2. The composition of claim 1 wherein the modifier composition is selected from the group consisting of anhydride-functional linseed oil, soya oil, tung oil, castor oil, sunflower oil, and other vegetable oils, anhydride-functional tall oil fatty acid, linseed fatty acid, soya fatty acid, dehydrated castor fatty acid, sunflower fatty acid, and mixtures thereof.
3. The composition of claim 1 wherein the isocyanate-functional material is selected from the group consisting of tetramethylene diisocyanate, hexamethylene diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 4,4'-diphenylmethane diisocyanate, isophorone diisocyanate, 4,4'-dicyclohexylmethane diisocyanate, benzene 1,3-bis(1-isocyanato-1-methylethyl), and mixtures thereof.
4. The composition of claim 1 wherein the catalyst is selected from the group consisting of di-butyl tin dilaurate, tin octoate and mixtures thereof.
5. The composition of claim 1 wherein between about 1% and about 10% by weight of the total polymer weight solids is contributed by diols and/or amines having ionic or hydrophilic groups which are contributed to the polyurethane-urea.
6. The composition of claim 5 wherein said diol and/or amines contain carboxylic acid groups, sulfonic acid groups, phosphoric acid groups, ammonium salts, phosphonium salts or sulfonium salts.
7. The composition of claim 1 wherein the diamine chain extender is present in an amount sufficient to react with up to about 90% of the theoretical amount of residual NCO functionality.
8. The composition of claim 1 wherein the isocyanate-functional prepolymer further comprises an active-hydrogen containing composition that is monofunctional with respect to isocyanates and which contains an aliphatic chain having at least six carbons.
9. The composition of claim 8 wherein from about 1% to about 50% of the total active hydrogen functionality of the prepolymer is contributed by the monofunctional composition.
10. The composition of claim 9 wherein the monofunctional composition is selected from the group consisting of hexyl, soya, tallow, hydrogenated tallow, stearyl, coco, lauryl, and oleyl alcohol, mercaptan, amine and mixtures thereof.
11. A composition comprising a dispersion of a polyurethane-urea in an aqueous media having a particle size diameter of less than about 0.4 micron; wherein the polyurethane-urea dispersion is obtained by dispersing, in the presence of a weak base, an isocyanate functional prepolymer into water and chain extending said prepolymer by admixing a (a) diamine chain extender and (b) a modifier composition selected from the group consisting of C6-C22 aliphatic chain-containing anhydride-functional fatty acids and oils, and mixtures thereof; wherein the prepolymer is obtained by reacting in the presence of a catalyst:
- (i) an active-hydrogen containing composition containing at least two active hydrogen groups per molecule;
- (ii) an isocyanate-functional material; and
12. The composition of claim 11 wherein the modifier composition is selected from the group consisting of anhydride-functional linseed oil, soya oil, tung oil, castor oil, sunflower oil, and other vegetable oils, anhydride-functional tall oil fatty acid, linseed fatty acid, soya fatty acid, dehydrated castor fatty acid, sunflower fatty acid, and mixtures thereof.
13. The composition of claim 11 wherein the isocyanate-functional material is selected from the group consisting of tetramethylene diisocyanate, hexamethylene diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 4,4'-diphenylmethane diisocyanate, isophorone diisocyanate, 4,4'-dicyclohexylmethane diisocyanate, benzene 1,3-bis(1-isocyanato-1-methylethyl), and mixtures thereof.
14. The composition of claim 11 wherein the catalyst is selected from the group consisting of di-butyl tin dilaurate, tin octoate and mixtures thereof.
15. The composition of claim 11 wherein between about 1% and about 10% by weight of the total polymer weight solids is contributed by diols and/or amines having ionic or hydrophilic groups which are contributed to the polyurethane-urea.
16. The composition of claim 15 wherein said diol and/or amines contain carboxylic acid groups, sulfonic acid groups, phosphoric acid groups, ammonium salts, phosphonium salts or sulfonium salts.
17. The composition of claim 11 wherein the diamine chain extender is present in an amount sufficient to react with up to about 90% of the theoretical amount of the residual NCO functionality.
18. The composition of claim 11 wherein the isocyanate-functional prepolymer further comprises an active-hydrogen containing composition that is monofunctional with respect to isocyanates and which contains an aliphatic chain having at least six carbons.
19. The composition of claim 18 wherein from about 1% to about 50% of the total active hydrogen functionality of the prepolymer is contributed by the monofunctional composition.
20. The composition of claim 19 wherein the monofunctional composition is selected from the group consisting of hexyl, soya, tallow, hydrogenated tallow, stearyl, coco, lauryl, and oleyl alcohol, mercaptan, amine and mixtures thereof.
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Type: Grant
Filed: Jun 7, 1995
Date of Patent: Jun 15, 1999
Assignee: The Sherwin-Williams Company (Cleveland, OH)
Inventors: Revathi R. Tomko (North Olmsted, OH), Barbara J. Varone (Munroe Falls, OH)
Primary Examiner: Rabon Sergent
Attorneys: Heidi A. Boehlefeld, Robert E. McDonald, Vivien Y. Tsang
Application Number: 8/474,292
International Classification: C08L 7502; C08L 7504; C08G 1830; C08G 1810;
